NOW APPROVED

JUVMO: a first-of-its-kind selective D1/D5 agonist1*

Man riding bike.
For the moments that move them.

*JUVMO is a selective partial agonist at the dopamine D1 and D5 receptor subtypes.1

AI-generated depiction. Not a real patient.

AI-generated depiction. Not a real patient.

PRESS PAUSE on oral levodopa increases with powerful, durable control1,2

In TEMPO-1, patients achieved improved motor symptom control (ADLs) without initiating oral levodopa at week 26.3 In TEMPO-3, patients experienced increased good "On" time while remaining on fixed oral levodopa doses at week 26.4

Powerful Efficacy & Durable Control1,2

Improvements in motor symptom control (ADLs) and good "On" time at week 26, observed through week 85

Demonstrated Safety1-5​

Consistent safety profile over 
85 weeks across 4 phase 3 clinical trials

Once-Daily Dosing1†


Once-daily dosing that can be taken with or without food and has a 24-hour half-life

†Please see Prescribing Information on dose modifications for CYP3A inducers and inhibitors.

93% of patients did not increase their oral levodopa dose after 85 weeks (TEMPO-4 OLE) with JUVMO + oral levodopa (96/103)6

Data are from TEMPO-3 active rollover patients. TEMPO-3 primary endpoint: Change in good "On" time without troublesome dyskinesia at week 26: +1.7 hours JUVMO + oral levodopa (N=242) vs +0.6 hours placebo + oral levodopa (N=245); P<0.0001.1

OLE Limitations: There is potential for enrichment of OLE data; unblinding patients may cause bias related to overall treatment effect; data are descriptive in nature, and findings should be interpreted with caution.

Man securing his bike to a bike rack.
Three adult friends riding bikes.

Ready to get your patients started on JUVMO?

ADLs=activities of daily living; OLE=open-label extension; PD=Parkinson's disease.